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features
design
support

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Write a Review

Description

Citeline serves as a robust platform for clinical development intelligence and analytics, offering life sciences organizations access to real-time research and development data, insights, and tools essential for making informed strategic choices throughout the drug and device development process. By compiling and refining the most comprehensive datasets related to global clinical trials, investigators, trial sites, drug development pipelines, and regulatory stipulations, it aids various functions including protocol design, feasibility assessments, selection of sites and investigators, enrollment predictions, competitive analysis, and tracking compliance with disclosure regulations in different jurisdictions. The platform encompasses several products, such as Pharmaprojects for monitoring drug pipelines, Trialtrove for benchmarking clinical trials, Sitetrove for gathering site and investigator intelligence, Global Patient Insights for ensuring feasibility aligns with actual patient access, and TrialScope Intelligence/Disclose for navigating regulatory disclosure requirements. With its wide range of functionalities, Citeline stands out as a vital resource for organizations aiming to streamline their clinical development processes and enhance their strategic decision-making capabilities. Moreover, the integration of these tools facilitates a more efficient approach to managing the complexities of clinical trials and regulatory compliance in an ever-evolving landscape.

Description

Jeeva's patent-pending modular system is built on the most powerful cloud platform. One login from any browser-enabled device can be used to remotely screen patients, educate, enroll, send SMS, email and generate evidence including electronic patient-reported outcomes. They are tired of waiting for patient recruitment and retention to happen. It is crucial to provide sufficient evidence of safety and efficacy for investigational new medicines in order to receive regulatory agency approval. Jeeva is a great tool for saving time and money for patients, biopharma sponsors, and long-term follow up studies for gene therapy.

API Access

Has API No 

API Access

Has API Yes 

Screenshots View All

Screenshots View All

Integrations

AWS Auto Scaling No 
AWS Backup No 
Django No 
GitHub No 
Google No 
Google Maps No 
Python No 
React Native No 
SendGrid No 
Twilio No 
Twilio Messaging No 
Twilio Voice No 
nOps No 

Integrations

AWS Auto Scaling Yes 
AWS Backup Yes 
Django Yes 
GitHub Yes 
Google Yes 
Google Maps Yes 
Python Yes 
React Native Yes 
SendGrid Yes 
Twilio Yes 
Twilio Messaging Yes 
Twilio Voice Yes 
nOps Yes 

Pricing Details

No price information available.
Free Trial No 
Free Version No 

Pricing Details

$100/mo/user
Indicated starting pricing is for academic and non-profit customers for a single software module subscription per study for users including patients.
Available for biopharma sponsors, CROs, and other organizations on a per trial basis or enterprise scale at most competitive pricing options based on geography, trial size, duration, type, standard or premium features.
Free Trial Yes 
Free Version Yes 

Deployment

Web-Based Yes 
On-Premises No 
iPhone App No 
iPad App No 
Android App No 
Windows No 
Mac No 
Linux No 
Chromebook No 

Deployment

Web-Based Yes 
On-Premises No 
iPhone App No 
iPad App No 
Android App No 
Windows No 
Mac No 
Linux No 
Chromebook No 

Customer Support

Business Hours Yes 
Live Rep (24/7) Yes 
Online Support Yes 

Customer Support

Business Hours Yes 
Live Rep (24/7) No 
Online Support Yes 

Types of Training

Training Docs Yes 
Webinars Yes 
Live Training (Online) Yes 
In Person No 

Types of Training

Training Docs No 
Webinars No 
Live Training (Online) Yes 
In Person Yes 

Vendor Details

Company Name

Citeline

Country

United States

Website

www.citeline.com

Vendor Details

Company Name

Jeeva Informatics Solutions

Founded

2019

Country

United States

Website

jeevatrials.com/solutions/

Product Features

Product Features

Clinical Trial Management

21 CFR Part 11 Compliance Yes 
Document Management No 
Electronic Data Capture Yes 
Enrollment Management Yes 
HIPAA Compliant Yes 
Monitoring Yes 
Patient Database Yes 
Recruiting Management Yes 
Scheduling Yes 
Study Planning Yes 

Electronic Data Capture

Audit Trail Yes 
CRF Tracking Yes 
Data Entry Yes 
Data Verification Yes 
Distributed Capture Yes 
Document Imaging No 
Document Indexing No 
Forms Management Yes 
Remote Capture Yes 
Study Management Yes 

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